NCT06784362

Brief Summary

The dental community, dental insurance companies and the public are becoming increasingly aware of the high prevalence of gum disease around teeth (periodontitis) and around dental implants (peri-implantitis). To date, it cannot be accurately predicted which individuals will develop or re-develop periodontitis or peri-implantitis, leading most dental patients to undergo unnecessary treatment and undue risks and costs. Gingival fluid is a serum-like fluid that diffuses into the oral cavity by flowing between the gum and the tooth or dental implant. Oral bacteria that grow around teeth and dental implants induce inflammation and change the amount and composition of the gingival fluid. The study hypothesizes that the spectra of metabolites in the inflammatory transudates and exudates around teeth and dental-implants are predictors of future periodontitis or peri-implantitis. The first objective is to use proton nuclear magnetic resonance (H-NMR) spectroscopy in a cross-sectional study to map mapping the metabolites in the gingival fluid that are capable of discriminating between healthy gum tissue and gum tissue that shows signs of periodontitis or dental peri-implantitis. The second objective is to begin prospective measurement of gingival fluid metabolites every 6 months in (i) individuals without periodontitis or peri-implantitis (healthy group), (ii) individuals with periodontitis or peri- implantitis who have been informed of the need for treatment - but have decided not to have treatment (untreated group) and (iii) individuals who received treatment for periodontitis or peri-implantitis and are now receiving regular dental hygiene care every 3 months (high risk group). By defining metabolites that can discriminate health from disease (Aim 1) and by measuring proportional changes of key metabolites relative to disease progression over time (Aim 2), the study will be able to predict in a site-specific manner, (a) the risk of disease initiation in people who do not initially have periodontitis or peri-implantitis (healthy persons), and (b) disease progression in untreated people or in people who were treated and are currently in a dental hygiene maintenance program. Accomplishing these two aims will provide a foundation from which to increase the efficacy of prevention whilst abating the morbidity and cost associated with current clinical practice.

Trial Health

100
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
230

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Dec 2016

Longer than P75 for all trials

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

December 5, 2016

Completed
7.2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 29, 2024

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

January 29, 2024

Completed
12 months until next milestone

First Submitted

Initial submission to the registry

January 14, 2025

Completed
6 days until next milestone

First Posted

Study publicly available on registry

January 20, 2025

Completed
Last Updated

January 20, 2025

Status Verified

January 1, 2025

Enrollment Period

7.2 years

First QC Date

January 14, 2025

Last Update Submit

January 14, 2025

Conditions

Outcome Measures

Primary Outcomes (2)

  • defining metabolites that can discriminate health from disease

    Gingival fluid samples using use proton nuclear magnetic resonance (H-NMR) spectroscopy, every 6 months for 24 months

    6, 12, 18, 24 months

  • measuring proportional changes of key metabolites relative to disease progression over time

    Gingival fluid samples using use proton nuclear magnetic resonance (H-NMR) spectroscopy, every 6 months for 24 months

    6, 12, 18, 24 months

Study Arms (3)

Healthy group

individuals without periodontitis or peri-implantitis

Other: No intervention

untreated group

individuals with periodontitis or peri- implantitis who have been informed of the need for treatment - but have decided not to have treatment (untreated group)

Other: No intervention

high risk group

individuals who received treatment for periodontitis or peri-implantitis and are now receiving regular dental hygiene care every 3 months (high risk group).

Other: No intervention

Interventions

This is an observational study

Healthy grouphigh risk groupuntreated group

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Subjects with disease (cases) were diagnosed with generalized chronic severe periodontitis with at least five teeth having clinical evidence of disease \[clinical attachment loss (CAL) ≥ 5mm and at least one site with probing depth (PD) ≥ 7 mm\], and radiographic evidence of at least 30% bone loss. Control subjects exhibited a healthy periodontium (no PD \>3 mm. no site with CAL) with no radiographic evidence of bone loss. Case and control subjects were in good general health. Smoking habits were noted. Case and control exclusion criteria included: 1) uncontrolled systemic disease, such as diabetes; 2) systemic antibiotic use within the past 3 months; 3) unable to provide consent; and 4) history of periodontal treatment or local antibiotic use in the past 12 months; 5) use of NSAIDs in the past 3 weeks.

You may qualify if:

  • Subjects with disease (cases) were diagnosed with generalized chronic severe periodontitis with at least five teeth having clinical evidence of disease \[clinical attachment loss (CAL) ≥ 5mm, at least one site with probing depth (PD) ≥ 7 mm\] and radiographic evidence of at least 30% bone loss
  • Control subjects exhibited a healthy periodontium (no PD \>3 mm. no site with CAL) with no radiographic evidence of bone loss.
  • Case and control subjects were in good general health.

You may not qualify if:

  • uncontrolled systemic disease, such as diabetes;
  • systemic antibiotic use within the past 3 months;
  • unable to provide consent; and
  • history of periodontal treatment or local antibiotic use in the past 12 months;
  • use of NSAIDs in the past 3 weeks.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Biospecimen

Retention: SAMPLES WITHOUT DNA

gingival fluid

MeSH Terms

Conditions

Periodontal DiseasesPeriodontitisPeri-Implantitis

Condition Hierarchy (Ancestors)

Mouth DiseasesStomatognathic Diseases

Study Design

Study Type
observational
Observational Model
CASE CONTROL
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

January 14, 2025

First Posted

January 20, 2025

Study Start

December 5, 2016

Primary Completion

January 29, 2024

Study Completion

January 29, 2024

Last Updated

January 20, 2025

Record last verified: 2025-01